← Back to Clinical Trials
Recruiting NCT07254195

NCT07254195 Assessment of an Intensive Motor Telerehabilitation Program for Stroke Patients

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07254195
Status Recruiting
Phase
Sponsor Hospices Civils de Lyon
Condition Stroke
Study Type INTERVENTIONAL
Enrollment 51 participants
Start Date 2026-02-25
Primary Completion 2028-01-25

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 85 Years
Study Type INTERVENTIONAL
Interventions
Telerehabilitation program using the MindMotion GO device

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 51 participants in total. It began in 2026-02-25 with a primary completion date of 2028-01-25.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Stroke is a major cause of motor disability, particularly hemiplegia, and its incidence is increasing as the population ages. Despite partial spontaneous recovery in the first three months, 80% of patients retain a motor deficit after six months, requiring intensive rehabilitation to maximize recovery. However, after hospitalization, access to intensive rehabilitation is limited, due to geographical and mobility constraints, and the lack of reimbursement for private occupational therapy. Telerehabilitation, using digital technologies, can overcome these difficulties by offering interactive, accessible rehabilitation at home. Studies show that its effectiveness is comparable to that of clinical rehabilitation. Our study therefore proposes to evaluate the feasibility and effects of a home-based telerehabilitation program using the MindMotion GO device (MindMaze). This 12-week program aims to provide an additional intensive dose of rehabilitation to the standard of care, with 300 minutes of weekly active therapy, planned and monitored remotely by a therapist.

Eligibility Criteria

Inclusion Criteria: * Hospitalized for a first ischemic or hemorrhagic stroke * Stroke occurrence more than 30 days prior * Presenting motor deficits affecting the upper limb, with or without involvement of the lower limb * Able to follow the instructions of the home program using the MindMotion GO device * Having at home an accessible email address, an Internet connection with password, a smartphone, a screen or TV with HDMI input (Full HD 1080p resolution), and a free space of approximately 1 m x 2.5 m in front of the screen * Ability to sit without assistance * Patient agreeing to participate in the study by signing an informed consent form * Affiliated with, or entitled to, a social security scheme Exclusion Criteria: History of stroke * Neurological pathology other than stroke * Patient with uncontrolled epilepsy or seizure disorder * Cardiac disease limiting exercise * Pain limiting rehabilitation dose * Major comprehension problems or severe psychiatric and/or cognitive disorders that could compromise understanding of the protocol and the smooth running of the study. * Uncorrected hearing or visual deficits * Severe apraxia * Severe memory impairment * Severe unilateral spatial neglect * Total plegia of affected limb * Pregnant, parturient or breast-feeding women * Persons deprived of their liberty by judicial or administrative decision * Persons admitted to a health or social institution for purposes other than research * Adults under legal protection (guardianship, curatorship) * Subjects participating in other intervention research.

Contact & Investigator

Central Contact

Jacques LUAUTÉ, MD

✉ Jacques.luaute@chu-lyon.fr

📞 4 78 86 50 64

Frequently Asked Questions

Who can join the NCT07254195 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 85 Years, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07254195 currently recruiting?

Yes, NCT07254195 is actively recruiting participants. Contact the research team at Jacques.luaute@chu-lyon.fr for enrollment information.

Where is the NCT07254195 trial being conducted?

This trial is being conducted at Saint-Genis-Laval, France.

Who is sponsoring the NCT07254195 clinical trial?

NCT07254195 is sponsored by Hospices Civils de Lyon. The trial plans to enroll 51 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology